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299 Possible Causes for Delayed Acquisition of Motor Skills, Mallory-Like Bodies, Mild Rib Sclerosis

  • Rigid Spine Syndrome

    Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion.[ncbi.nlm.nih.gov] bodies; desmin-related myopathy with Mallory body-like inclusions; early-onset desmin-related myopathy; Eichsfeld type congenital muscular dystrophy; MDRS1; rigid spine syndrome[informatics.jax.org] bodies desmin-related myopathy with Mallory body-like inclusions early-onset desmin-related myopathy Eichsfeld type congenital muscular dystrophy MDRS1 rigid spine syndrome[familydiagnosis.com]

    Missing: Mild Rib Sclerosis
  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    body-like inclusions Desminopathy Developmental and speech delay due to SOX5 deficiency Developmental delay with autism spectrum disorder and gait instability Developmental[se-atlas.de] Dejerine-Sottas syndrome Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome Dentatorubral pallidoluysian atrophy Dermatomyositis Desmin-related myopathy with Mallory[se-atlas.de]

    Missing: Mild Rib Sclerosis
  • Congenital Muscular Dystrophy with Integrin Alpha-7 Deficiency

    Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion, although[invitae.com] […] a subtype of desmin-related myopathies, which also shows Mallory body-like inclusions.[scielo.br] Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion.[ncbi.nlm.nih.gov]

    Missing: Mild Rib Sclerosis
  • Muscular Dystrophy-Dystroglycanopathy Type B6

    Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion.[ncbi.nlm.nih.gov] body-like inclusions.[ncbi.nlm.nih.gov] Poor or decreased motor abilities, delay or arrest of motor milestones, and joint or spinal deformities are often the presenting features of CMD.[ncbi.nlm.nih.gov]

    Missing: Mild Rib Sclerosis
  • Muscular Dystrophy-Dystroglycanopathy Type B5

    Since delay of motor skill acquisition may be a presenting symptom of CMD, onset of manifestations before age two years may be a reasonable diagnostic criterion.[ncbi.nlm.nih.gov] body-like inclusions.[ncbi.nlm.nih.gov] Poor or decreased motor abilities, delay or arrest of motor milestones, and joint or spinal deformities are often the presenting features of CMD.[ncbi.nlm.nih.gov]

    Missing: Mild Rib Sclerosis
  • Congenital Myopathy with Excess of Thin Filaments

    Respective terms such as cytoplasmic bodies, Mallory body-like inclusions or granulofilamentous material, earlier marking certain CM, only entered the group of PAM when immunohistochemistry[bioline.org.br] Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Muscle Nerve 1983;6:195-200. Back to cited text no. 14 [ PUBMED ] 15.[bioline.org.br] Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene. Ann Neurol 2004;55:676-86. Back to cited text no. 15 16.[bioline.org.br]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive Centronuclear Myopathy

    body-like inclusions Duane anomaly, myopathy, scoliosis syndrome Duane's syndrome Duane's syndrome, type 3 Hereditary progressive muscular dystrophy Inclusion body myopathy[icdlist.com] […] with fiber type disproportion Congenital myopathy with uniform fiber type Congenital nonprogressive myopathy with Moebius and Robin sequences Desmin related myopathy with Mallory[icdlist.com]

    Missing: Mild Rib Sclerosis
  • Autosomal Recessive Spastic Paraplegia Type 56

    body-like inclusions Distal hereditary motor neuropathy type 7 Distal monosomy 15q Distal myopathy with vocal cord weakness Donnai-Barrow syndrome Early-onset myopathy with[csbg.cnb.csic.es] Craniofacial-deafness-hand syndrome Craniofrontonasal dysplasia Craniorachischisis Deafness - lymphedema - leukemia Dejerine-Sottas syndrome Desmin-related myopathy with Mallory[csbg.cnb.csic.es]

    Missing: Mild Rib Sclerosis
  • Achondroplasia

    Spine radiograph lateral view (b) demonstrating mild platyspondyly and expansion of anterolateral parts of the ribs with “club-shaped” configuration (arrows).[doi.org] The changes involve areas of bone sclerosis intermingled with areas of resorption.[doi.org]

    Missing: Mallory-Like Bodies
  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    body-like inclusions Desminopathy Developmental and speech delay due to SOX5 deficiency Developmental delay with autism spectrum disorder and gait instability Developmental[se-atlas.de] Dejerine-Sottas syndrome Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome Dentatorubral pallidoluysian atrophy Dermatomyositis Desmin-related myopathy with Mallory[se-atlas.de]

    Missing: Mild Rib Sclerosis